A Case of Lipoprotein Lipase Deficiency inan Infant with Recurrent Pancreatitis / 대한소아소화기영양학회지
Korean Journal of Pediatric Gastroenterology and Nutrition
;
: 79-83, 2009.
Artículo
en Coreano
| WPRIM
| ID: wpr-25026
ABSTRACT
Familial chylomicronemia syndrome is a rare disorder characterized by severe hypertriglyceridemia and fasting chylomicronemia. Causes of the syndrome include lipoprotein lipase (LPL) deficiency, apolipoprotein C-II deficiency, or the presence of inhibitors to LPL. We managed a 3-month-old girl who had recurrent acute pancreatitis caused by chylomicronemia. We report the first case of familial chylomicronemia in Korea caused by LPL deficiency in an infant with recurrent acute pancreatitis.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Pancreatitis
/
Hipertrigliceridemia
/
Ayuno
/
Corea (Geográfico)
/
Lipoproteína Lipasa
/
Hiperlipoproteinemia Tipo I
/
Lipoproteínas
Límite:
Humanos
/
Lactante
País/Región como asunto:
Asia
Idioma:
Coreano
Revista:
Korean Journal of Pediatric Gastroenterology and Nutrition
Año:
2009
Tipo del documento:
Artículo
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